Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
291
datasets available to search
ShareScore release 0.9.0
Dataset results
291 results for “Genetic variants”
Clock and Narcolepsy Genetic Variants and the Effects of Stalevo® (Levodopa/Carbidopa/Entacapone) on Sleep Disorders in Parkinson's Disease
ClinicalTrials.gov study NCT02452606. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Genetic Copy Number Variants in Sib Pairs Both Affected with Schizophrenia
GEO Series GSE16930. Homo sapiens. 20 samples. Type: Genome variation profiling by array.
Global discovery of SLE genetic risk variant allelic enhancer activity
GEO Series GSE143792. Homo sapiens; unidentified plasmid. 25 samples. Type: Expression profiling by high throughput sequencing; Other.
Functional Schizophrenia-associated genetic variant near the TSNARE1 and ADGRB1 genes
GEO Series GSE263894. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
Germline and somatic genetic variants in the p53 pathway interact to affect cancer risk, progression, and drug response
GEO Series GSE143561. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Systematic Evaluation Of Genes And Genetic Variants Associated With Type 1 Diabetes Susceptibility
GEO Series GSE77350. Homo sapiens. 590 samples. Type: Expression profiling by array.
Genetic effects on liver chromatin accessibility identify disease regulatory variants [RNA-seq]
GEO Series GSE164876. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing.
Identification of Genetic Variants Contributing to Cisplatin-Induced Cytotoxicity using a Genome-wide Approach
GEO Series GSE7761. Homo sapiens. 176 samples. Type: Expression profiling by array.
Functional Validation of Common Idiopathic Pulmonary Fibrosis Genetic Risk Variants [850k methylation arrays]
GEO Series GSE175458. Homo sapiens. 547 samples. Type: Methylation profiling by genome tiling array.
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbance
GEO Series GSE195873. Homo sapiens. 18 samples. Type: Methylation profiling by genome tiling array.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell [RNA-Seq]
GEO Series GSE205281. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell
GEO Series GSE205293. Homo sapiens. 17 samples. Type: Expression profiling by high throughput sequencing; Other.
Scalable generation and functional classification of genetic variants in inborn errors of immunity to accelerate clinical diagnosis and treatment
GEO Series GSE298853. Homo sapiens. 24 samples. Type: Other.
Massively parallel reporter assays investigate shared genetic variants of eight psychiatric disorders
GEO Series GSE244011. Homo sapiens. 44 samples. Type: Other.
Identification of genetic variants affecting vitamin D receptor binding and associations with autoimmune disease
GEO Series GSE73254. Homo sapiens. 30 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Fucntional genetic variants mediate their regulatory effects through altered transcription factor binding. [Bisulfite-Seq]
GEO Series GSE117565. Homo sapiens. 17 samples. Type: Methylation profiling by high throughput sequencing.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell [MGA-Seq]
GEO Series GSE205286. Homo sapiens. 11 samples. Type: Other.
Genetic variants alter T-bet binding and gene expression in mucosal inflammatory disease
GEO Series GSE81881. Homo sapiens. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Promoter sequence and architecture determine expression variability and confer robustness to genetic variants [GM12878]
GEO Series GSE188099. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Genetic Variants of Phospholipase C-γ2 Confer Altered Microglial Phenotypes and Differential Risk for Alzheimer’s Disease.
GEO Series GSE237495. Mus musculus. 30 samples. Type: Expression profiling by high throughput sequencing.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.